Canonical Allele Identifier: CA14915802
Gene: IFNAR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33354946T>G , CM000683.2:g.33354946T>G GRCh38
NC_000021.8:g.34727252T>G , CM000683.1:g.34727252T>G GRCh37
NC_000021.7:g.33649122T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000442071.3:c.1144-370T>G ENSP00000400161.3:n.1144-370T>G
ENST00000651609.2:c.*1158-370T>G ENSP00000498594.1:n.*1158-370T>G
ENST00000652450.2:c.1234-370T>G ENSP00000498654.1:n.1234-370T>G
ENST00000652654.3:c.*899-370T>G ENSP00000498666.1:n.*899-370T>G
ENST00000700046.1:c.*1028-370T>G ENSP00000514762.1:n.*1028-370T>G
ENST00000700080.1:c.1234-370T>G ENSP00000514785.1:n.1234-370T>G
ENST00000700084.1:c.679-370T>G ENSP00000514786.1:n.679-370T>G
ENST00000700085.1:n.2105-370T>G
ENST00000700086.1:n.1442-370T>G
ENST00000703514.1:c.*642-370T>G ENSP00000515347.1:n.*642-370T>G
ENST00000703515.1:c.1441-370T>G ENSP00000515348.1:n.1441-370T>G
ENST00000703516.1:c.*764-370T>G ENSP00000515349.1:n.*764-370T>G
ENST00000703556.1:c.1441-370T>G ENSP00000515372.1:n.1441-370T>G
ENST00000703557.1:c.1441-385T>G ENSP00000515373.1:n.1441-385T>G
ENST00000703561.1:c.1144-2769T>G ENSP00000515377.1:n.1144-2769T>G
ENST00000703562.1:c.*910-370T>G ENSP00000515378.1:n.*910-370T>G
ENST00000703563.1:c.*1028-370T>G ENSP00000515379.1:n.*1028-370T>G
ENST00000703564.1:c.*1158-370T>G ENSP00000515380.1:n.*1158-370T>G
ENST00000703565.1:c.*316-370T>G ENSP00000515381.1:n.*316-370T>G
ENST00000270139.8:c.1441-370T>G MANE Select ENSP00000270139.3:n.1441-370T>G
ENST00000652450.1:c.1234-370T>G ENSP00000498654.1:n.1234-370T>G
ENST00000270139.7:c.1441-370T>G ENSP00000270139.3:n.1441-370T>G
NM_000629.2:c.1441-370T>G NP_000620.2:n.1441-370T>G
XM_005260964.1:c.1234-370T>G XP_005261021.1:n.1234-370T>G
XM_005260964.2:c.1234-370T>G XP_005261021.1:n.1234-370T>G
NM_000629.3:c.1441-370T>G MANE Select NP_000620.2:n.1441-370T>G
NM_001384498.1:c.1441-370T>G NP_001371427.1:n.1441-370T>G
NM_001384499.1:c.1295-370T>G NP_001371428.1:n.1295-370T>G
NM_001384500.1:c.679-370T>G NP_001371429.1:n.679-370T>G
NM_001384501.1:c.1426-385T>G NP_001371430.1:n.1426-385T>G
NM_001384502.1:c.979-370T>G NP_001371431.1:n.979-370T>G
NM_001384503.1:c.1441-385T>G NP_001371432.1:n.1441-385T>G
NM_001384504.1:c.1234-370T>G NP_001371433.1:n.1234-370T>G